Home/Recalls/CANADA-57449
Health CanadaType III

System DI-60 Main Unit and Remore Review Software (2017-07-27)

Published: September 5, 2017Recall ID: 57449Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

System DI-60 Main Unit and Remore Review Software (2017-07-27)

Additional Source Details

FieldValue
N I D57449
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/system-di-60-main-unit-and-remore-review-software-2017-07-27
IssueMedical devices
Title System DI-60 Main Unit and Remore Review Software (2017-07-27)
Archived1
CategoryMedical devices
Last updated2017-09-05
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert